iconplc - United States, IT - Administration

ICON seeks a Director, Research Services, Oncology to lead clinical research in Blue Bell, PA. This role drives protocol development, study start-up, and regulatory submissions (FDA/EMA) for solid tumor programs. Requires 8+ years oncology experience, a life sciences degree (Pharm.D./Ph.D. prefer...

Join ICON plc as a CRA II or Senior CRA in a home-based role across the U.S. (Portland, Salt Lake City, Houston, Downers Grove, Lawrence). You will independently monitor clinical trials, ensure ICH-GCP compliance, and safeguard data integrity. Requires a Bachelor’s degree, 1-3+ years of monitorin...

Senior Manager, Regulatory Strategy role in Raleigh, US. Leverage 7+ years of regulatory expertise to design clinical trials, develop submission plans, and advise ICON clients. Requires a Bachelor's in science/healthcare, supervisory experience, and strong strategic drug development skills. Benef...

Join ICON plc as a Clinical Associate (CTA) in Blue Bell, PA, and support cutting-edge clinical trials. Leverage your scientific degree and CRO experience to coordinate study activities, ensure regulatory compliance, and drive data accuracy. Enjoy competitive benefits including health insurance, ...

Seeking an experienced **Project and Portfolio Manager** in **Blue Bell, PA** to lead large-scale programs and cross-functional teams. You will drive complex projects from planning to delivery, managing budgets, resources, and risk. Requires a Bachelor’s degree, proven program management success,...

Senior Clinical Research Associate sought for a dynamic role at ICON, overseeing global trials with a focus on ophthalmology or gene therapy. Requires 5+ years of CRA experience, deep ICH-GCP knowledge, and 60% travel. Drive site management, ensure data integrity, and advance innovative treatment...

ICON plc seeks a Country Lead Monitor in Raleigh, NC, to drive clinical trial operations. You will manage study deliverables, ensure regulatory compliance, and build stakeholder relationships. Requires a science degree, therapeutic expertise, and prior monitoring experience. Enjoy competitive ben...

Lead and coordinate clinical trial projects as a Trial Delivery Manager at ICON in Blue Bell, PA. We seek a seasoned project management professional with a Bachelor’s degree and proven leadership skills to deliver results on time and within budget. Drive cross-functional teams, manage stakeholder...

Senior Clinical Research Associate needed for Neurovascular trials in the Central/Midwest US. Monitor complex studies onsite or remotely, ensuring ICH-GCP and FDA compliance. Requires a BS in Life Sciences, 3+ years of CRO/pharma monitoring experience, and strong problem-solving skills. Enjoy com...

Senior Clinical Trial Manager (Oncology) – Home-Based, Blue Bell, US. Lead end-to-end trial management as a site-aligned partner, driving communication and issue resolution. Requires 3-5+ years of trial management, solid tumor oncology expertise, and ICH-GCP knowledge. Enjoy competitive benefits,...

ICON plc seeks a Clinical Research Associate II (XTA) in Chicago. Leverage 2+ years of on-site monitoring experience across multiple therapeutic areas. Ensure site compliance with ICH-GCP and manage visits using CTMS/eTMF. Enjoy competitive benefits, annual leave, and up to 50% travel across the ...